Informations générales (source: ClinicalTrials.gov)
Controlled Education Of Patients After Stroke (CEOPS)
Interventional
N/A
University Hospital, Lille (Voir sur ClinicalTrials)
janvier 2014
juillet 2021
29 juin 2024
The main objective of the study is to compare the benefit of optimised follow-up by
nursing personnel from the vascular neurology department, including therapeutic follow-up
and an educational program directed to the patient and a caregiving member of his social
circle, with that of a typical follow-up.
Etablissements
Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
---|---|---|---|---|---|
GH PARIS SITE SAINT JOSEPH | MATHIEU ZUBER, MD phd | Contact (sur clinicalTrials) | |||
Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
C H U Dupuytren Limoges - Limoges - France | Contact (sur clinicalTrials) | ||||
CH - 62100 - Calais - France | OLIVIER DEREEPER, MD | Contact (sur clinicalTrials) | |||
Ch Intercommunal Compiègne-Noyon - Compiegne - Compiègne - France | Contact (sur clinicalTrials) | ||||
Ch Sambre Avesnois Maubeuge - Maubeuge - France | Contact (sur clinicalTrials) | ||||
Chru Nancy - Hopitaux de Braboi - Vandœuvre-lès-Nancy - France | Contact (sur clinicalTrials) | ||||
CHU - 25000 - Besancon - France | THIERRY MOULIN, MDphD | Contact (sur clinicalTrials) | |||
CHU - 33076 - Bordeaux - France | IGOR SIBON, MD phD | Contact (sur clinicalTrials) | |||
CHU - 76031 - Rouen - France | EVELYNE MASSARDIER, MD | Contact (sur clinicalTrials) | |||
Chu de Grenoble Alpes - Grenoble 9 - Grenoble - France | Contact (sur clinicalTrials) | ||||
Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
CHRU - 59037 - Lille - France | REGIS BORDET, MD phD | Contact (sur clinicalTrials) | |||
Chru Brest - Brest - France | Contact (sur clinicalTrials) | ||||
CHU - 21000 - Dijon - France | MAURICE GIROUD, MD phD | Contact (sur clinicalTrials) | |||
Chu Amiens Picardie - Amiens - France | Contact (sur clinicalTrials) | ||||
Chu La Miletrie - Poitiers - Poitiers - France | Contact (sur clinicalTrials) | ||||
Hopital Pierre Wertheimer - Hcl - Bron - France | Contact (sur clinicalTrials) | ||||
Samsah Ghicl Capinghem - Capinghem - France | Contact (sur clinicalTrials) |
Critères
Tous
Inclusion Criteria:
- Patients over 60 years of age
- Patients who have had a first stroke, transient or permanent, ischaemic or
haemorrhagic, justifying hospitalisation
- Patients with high blood pressure already treated or discovered at the time of the
stroke and justifying the start of a treatment
- Patients who have had a stroke with sequelae allowing immediate return home or
justifying a stay of less than one month in rehabilitation
- Patient having a member of his social circle who has agreed to provide follow-up for
two years in association with the assigned nursing personnel in case of
randomisation into the "optimised follow-up" group.
Exclusion criteria
- Patients less than 60 years of age
- Patients with a history of stroke
- Patients who do not have high blood pressure discovered by a treatment prior to the
stroke or by abnormal blood pressure figures during hospitalisation
- Patients who have had a stroke causing serious sequelae, justifying an extended stay
in a rehabilitation department
- Patient who has no one in his social circle capable of working with the assigned
nursing personnel, or patient living in an institution
- Patients over 60 years of age
- Patients who have had a first stroke, transient or permanent, ischaemic or
haemorrhagic, justifying hospitalisation
- Patients with high blood pressure already treated or discovered at the time of the
stroke and justifying the start of a treatment
- Patients who have had a stroke with sequelae allowing immediate return home or
justifying a stay of less than one month in rehabilitation
- Patient having a member of his social circle who has agreed to provide follow-up for
two years in association with the assigned nursing personnel in case of
randomisation into the "optimised follow-up" group.
Exclusion criteria
- Patients less than 60 years of age
- Patients with a history of stroke
- Patients who do not have high blood pressure discovered by a treatment prior to the
stroke or by abnormal blood pressure figures during hospitalisation
- Patients who have had a stroke causing serious sequelae, justifying an extended stay
in a rehabilitation department
- Patient who has no one in his social circle capable of working with the assigned
nursing personnel, or patient living in an institution